Download Delton Fingertip Oximeter User manual

Fingertip
Pulse Oximeter
Front Panel
RMI-POX2D
USER MANUAL
Ver2.0C204
General Description
Oxygen Saturation is a percentage of Oxyhemoglobin (HbO2) capacity, compounded with oxygen, by all combinative hemoglobin
(Hb) capacity in blood. In other words, it is consistency of Oxyhemoglobin in blood. It is a very important parameter for the
Respiratory Circulation System. Many respiratory diseases can result in oxygen saturation being lowered in human blood.
Additionally, the following factors can reduce oxygen saturation: Automatic regulation of organ dysfunction caused by Anesthesia,
Intensive Postoperative Trauma, injuries caused by some medical examinations. That situation might result in light-headedness,
asthenia, and vomiting. Therefore, it is very important to know the oxygen saturation of a patient so that doctors can find problems
in a timely manner.
The fingertip pulse oximeter features low power consumption, convenient operation and portability. Place one fingertip into the
photoelectric sensor for diagnosis and the pulse rate and oxygen saturation will appear on the display. It has been proven in clinical
experiments that it also features high precision and repeatability.
Measurement Principle
Diagram of Operation Principle
1. Red and Infrared-ray Emission Tube
2. Red and Infrared-ray Receipt Tube
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Before use, carefully read the manual.
Operation of the fingertip pulse oximeter may be affected by the use of an electrosurgical unit (ESU).
The fingertip pulse oximeter must be able to measure the pulse properly to obtain an accurate SpO2 measurement. Verify
that nothing is hindering the pulse measurement before relying on the SpO2 measurement.
Do not use the fingertip pulse oximeter in an MRI or CT environment.
Do not use the fingertip pulse oximeter in situations where alarms are required. The device has no alarms. It is not for
continuous monitoring.
Do not use the fingertip pulse oximeter in an explosive atmosphere.
The fingertip pulse oximeter is intended only as an adjunct in patient assessment. It must be used in conjunction with other
methods of assessing clinical signs and symptoms.
Check the pulse oximeter sensor application site every 4 hours to determine the positioning of the sensor and circulation
and skin sensitivity of the patient.
Do not sterilize the device using autoclaving, ethylene oxide sterilizing, or immersing the device in liquid. The device is not
intended for sterilization.
Follow local ordinances and recycling instructions regarding disposal or recycling of the device and device components,
including batteries.
This equipment complies with IEC 60601-1-2:2007 for electromagnetic compatibility for medical electrical equipment and/or
systems. However, because of the proliferation of radio-frequency transmitting equipment and other sources of electrical
noise in healthcare and other environments, it is possible that high levels of such interference due to close proximity or
strength of a source might disrupt the performance of this device.
Portable and mobile RF communications equipment can affect medical electrical equipment.
Inaccurate measurements may be caused by
Significant levels of dysfunctional hemoglobin (such as carbonyl - hemoglobin or methemoglobin);
Intravascular dyes such as indocyanine green or methylene blue;
High ambient light. Shield the sensor area if necessary;
Excessive patient movement;
High-frequency electrosurgical interference and defibrillators;
Venous pulsations;
Placement of a sensor on an extremity with a blood pressure cuff, arterial catheter, or intravascular line;
The patient has hypotension, severe vasoconstriction, severe anemia, or hypothermia;
The patient is in cardiac arrest or is in shock;
Fingernail polish or false fingernails;
Weak pulse quality (low perfusion);
Low hemoglobin;
Product Properties
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2.
Install two AAA batteries into the battery compartment. Match the plus (+) and minus (-)
signs in the compartment. If the polarities are not matched, damage may be caused to
the oximeter.
Slide the battery door cover horizontally along the arrow shown as the picture.
Notes:
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Install the batteries in right polarity. Incorrect placement may cause damage to the
bracket.
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Please remove the batteries if the pulse oximeter will not be used for long periods of time.
Using the Lanyard
Rx only: “Caution: Federal law (USA) restricts this device to sale by or on the order of a licensed practitioner.”
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One lanyard
Two AAA batteries
One instruction manual
Battery Installation
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2.
Precautions For Use
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Product Accessories
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Principle of the oximeter is as follows: A mathematical formula is established making use of Lambert Beer Law according to
Spectrum Absorption Characteristics of Reductive hemoglobin(RHb) and Oxyhemoglobin (HbO2) in glow and near-infrared zones.
Operation principle of the instrument: Photoelectric Oxyhemoglobin Inspection Technology is adopted in accordance with Capacity
Pulse Scanning and Recording Technology, so that two beams of different wavelength of lights (660nm glow and 940nm near
infrared light) can be focused onto a human nail tip through a clamping finger-type sensor. A measured signal obtained by a
photosensitive element, will be shown on the oximeter’s display through process in electronic circuits and microprocessor shown on
the oximeter’s display through electronic circuits and a microprocessor.
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Patient pulse quality signals are indicated by bar graph. The bar is graded as 10 levels, if the strength is level 2 to 3, the pulse signal
is inadequate.
Operation of the product is simple and convenient.
The product is small in volume, light in weight and convenient to carry.
Power consumption of the product is low and the two AAA batteries can be operated continuously for 30 hours.
A low voltage warning will be indicated when battery voltage is low and normal operation of the oximeter might be influenced.
The product will automatically power off when there is no signal for longer than 8 seconds.
Intended Use
Fingertip pulse oximeter is a portable non-invasive device intended for spot-checking of oxygen saturation of arterial hemoglobin
(SpO2) and pulse rate of adult and pediatric patient at home, and hospital (including clinical use in internist/surgery, Anesthesia,
intensive care etc). It is not for continuous monitoring.
Thread thinner end of the lanyard through the hanging hole.
Thread thicker end of the lanyard through the threaded end before pulling it
tightly.
Warnings!
1.
Keep the oximeter away from young children. Small items such as the battery door,
battery, and lanyard are choking hazards.
2.
Do not hang the lanyard from the device’s electrical wire.
Maintenance and Storage
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Replace the batteries in a timely manner when low voltage lamp is lighted.
Clean surface of the fingertip oximeter before it is used in diagnosis for patients.
Remove the batteries if the oximeter is not operated for a long time.
It is best to store the product in -20℃～+55℃ and ≤93% humidity.
Keep in a dry place. Extreme moisture may affect oximeter lifetime and may cause damage.
Dispose of battery properly; follow any applicable local battery disposal laws.
Cleaning the fingertip pulse oximeter
Please use medical alcohol to clean the silicone touching the finger inside of oximeter with a soft cloth dampened with 70%
isopropyl alcohol. Also clean the being tested finger using alcohol before and after each test.
Do not pour or spray liquids onto the oximeter, and do not allow any liquid to enter any openings in the device. Allow the oximeter to
dry thoroughly before reuse.
A functional tester cannot be used to assess the accuracy of a pulse oximeter monitor or sensor. Clinical testing is used to establish
the SpO2 accuracy. The measured arterial hemoglobin saturation value (SpO2) of the sensors is compared to arterial hemoglobin
oxygen (SaO2) value, determined from blood samples with a laboratory CO-oximeter. The accuracy of the sensors in comparison to
the CO-oximeter samples measured over the SpO2 range of 70 – 100%. Accuracy data is calculated using the
root-mean-squared (Arms value) for all subjects, per ISO 9919:2005, Medical Electrical Equipment–Particular requirements for the
basic safety and essential performance of pulse oximeter equipment for medical use.
Specifications
1. Display Type
OLED display
Data update time: <2s
2. SpO2
Display range: 0-99%
Measurement range: 70-99%
Accuracy: 70%-99%: ±3%; 0%~69% no definition
Resolution: 1%
3. Pulse Rate
Display range: 0~254BPM
Measure range: 30-235 BPM
Accuracy: 30~99bpm, ±2bpm; 100~235bpm, ±2%
Resolution: 1BPM
4. LED Wavelengths
Probe LED Specifications
Wavelength
The fingertip pulse oximeter requires no routine calibration or maintenance other than replacement of batteries.
Operation Instructions
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Install two AAA batteries according to the Battery Installation instructions listed above in the right column.
Open the clamp as illustrated in the picture below.
Fully insert one fingertip into the silicone hole of the oximeter before releasing the clamp.
Press the switch button once on front panel.
Keep your finger still during measurement.
Read corresponding data from display screen.
Press the button again to toggle between two display modes.
After turning on the Oximeter, each time you press the power switch, the Oximeter will switch to another display mode.
There are 2 display modes shown as follows:
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2.
Holding the power switch for longer than one second, will adjust the brightness of the oximeter. There are 10 levels of brightness.
The default level is level four.
Radiant Power
RED
660±2nm
1.8mW
IR
940±10nm
2.0mW
5. Power Requirements
Two AAA alkaline Batteries
Power consumption: Less than 40mA
Battery Life: Two AAA 1.5V, 600mAh alkaline batteries could be continuously operated as long as 30 hours.
It is equipped with a function switch, through which the oximeter can be powered off in case no finger is the oximeter longer than 8
seconds.
6. Outline Dimension
Length: 58mm
Width: 32mm
Height: 34mm
Weight: 50g (including two AAA batteries)
7. Environment Requirements
Operation Temperature: 5～40℃
Storage Temperature: -20～+55℃
Ambient Humidity: 15%~80% in operation
≤93% in storage
8. Equipment Response Time
As shown in the right figure.
Response time of slower average is 9.1s.
The Pulse Oximeter (RMI-POX2D) is intended for use in electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the Pulse Oximeter (RMI-POX2D) can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Pulse
Oximeter (RMI-POX2D) as recommended below, according to the maximum output power of the communications equipment.
Rated
maximum
output
Separation distance according to frequency of transmitter (m)
power of transmitter (W)
800 MHz to 2.5 GHz
80 MHz to 800 MHz
0.01
0.1167
0.2334
0.1
0.3689
0.7378
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1.1667
2.3334
10
3.6893
7.3786
100
11.6667
23.3334
For transmitters rated at a maximum output power not listed above, the recommended separation distanced in meters (m) can
be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of
the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.
Declaration
Guidance and Manufacturer’s declaration – electromagnetic emissions-For all EQUIPMENT and SYSTEMS
Guidance and Manufacturer’s declaration - electromagnetic emission
The RMI-POX2D Pulse Oximeter is intended for use in the electromagnetic environment specified below. The customer or the
user of RMI-POX2D Pulse Oximeter should assure that it is used in such an environment.
Emission test
RF emissions CISPR 11
Compliance
Group 1
RF emissions CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/ flicker emissions
IEC 61000-3-3
Class B
Not Applicable
Not Applicable
Electromagnetic Environment – guidance
The RMI-POX2D Pulse Oximeter uses RF energy only for
its internal function. Therefore, its RF emissions are very
low and are not likely to cause any interference in nearby
electronic equipment.
The pulse Oximeter (RMI-POX2D) is suitable for use in all
establishment, including domestic establishments and
those directly connected to the public low-voltage power
supply network that supplies buildings used for domestic
purposes.
Guidance and Manufacturer’s declaration – electromagnetic immunity-For all EQUIPMENT and SYSTEMS
Guidance and Manufacturer’s declaration - electromagnetic immunity
The RMI-POX2D Pulse Oximeter is intended for use in the electromagnetic environment specified below. The customer or the
user of the RMI-POX2D Pulse Oximeter should assure that it is used in such an environment.
Immunity test
IEC 60601 test
Compliance
Electromagnetic Environment – guidance
level
Level
Electrostatic
+/- 6kV contact
+/- 6kV contact
Floors should be wood, concrete or ceramic tile. If
Discharge (ESD)
+/- 8kV air
+/- 8kV air
floor are covered with synthetic material, the relative
IEC 61000-4-2
humidity should be at least 30%.
Power frequency (50/60 Hz)
3A/m
3A/m
Power frequency magnetic fields should be at levels
magnetic field
characteristics of a typical location in a typical
IEC 61000-4-8
commercial or hospital environment.
Possible Problems and Solutions
Problems
SpO2 or PR can not
be shown normally
SpO2 or PR is shown 1. Finger might not be inserted deep enough.
2. Excessive patient movement
unstably
The oximeter can not 1. No battery or low power of battery
2. Batteries might be installed incorrectly
be powered on
3. The oximeter might be damaged
Indication lamps are
suddenly off
“Error3” or
“Error4” is displayed
on screen
Error 6
“Error7” is displayed
on screen
Guidance and Manufacturer’s declaration - electromagnetic immunity
The RMI-POX2D Pulse Oximeter is intended for use in the electromagnetic environment specified below. The customer or the
user of the RMI-POX2D Pulse Oximeter should assure that it is used in such an environment.
Immunity
IEC
60601
Compliance
Electromagnetic Environment – guidance
test
test level
Level
Portable and mobile RF communications equipment should be used no closer
to any part of the Pulse Oximeter (RMI-POX2D), including cables, than the
recommended separation distance calculated from the equation applicable to
the frequency of the transmitter.
Recommended separation distance
3 V/m
3 V/m
Radiated
RF
80 MHz to
IEC
2.5 GHz
1. The product is automatically powered off when no
signal is detected longer than 8 seconds
2. The battery power is too low to work
1. Err 3 means the red emission LED is damaged
2. Err 4 means the infra-red emission LED is damaged
Solution
1. Retry by inserting the finger
2. There is excessive illumination
3. Try some more times. If you can make sure no
problem is existing in the product, please go
to a hospital timely for exact diagnosis.
1. Retry by inserting the finger
2. Be calmness
1. Please replace batteries
2. Please reinstall the batteries
3. Please contact with local customer service
centre
1. Normal
2. Replace the batteries
1. Check the red emission LED
2. Check the infra-red emission LED
Err 6 means the screen is failure
Change the screen
Err 7 means all the emission LED or reception dioxide is Check the emission LED and reception dioxide.
damaged.
Symbol Definitions
Symbol
Definition
Type BF applied part.
Attention, consult accompanying documents.
Protected against dripping water.
Guidance and Manufacturer’s declaration – electromagnetic immunityFor all EQUIPMENT and SYSTEMS that are not LIFE-SUPPORTING
Possible reason
1. Finger is not inserted correctly
2. Patient’s SpO2 value is too low to be measured
﹪SpO2
Oxygen saturation
PR bpm
Pulse rate (BPM)
Low power indication
No SpO2 Alarm
SN
Serial No.
Storage temperature and relative humidity
80 MHz to 800 MHz
Date of Manufacture
61000-4-3
800 MHz to 2.5 GHz
Where P is the maximum output power rating of the transmitter in watts (W)
according to the transmitter manufacturer and d is the recommended
separation distance in meters (m).
Field strengths from fixed RF transmitters, as determined by an
electromagnetic site surveya, should be less than the compliance level in each
frequency range. b
Interference may occur in the vicinity of equipment marked with following
symbol:
Note: The illustrations used in this manual may differ slightly from the appearance of the actual product.
Manufactured for:
Roscoe Medical, Inc.
21973 Commerce Parkway
Strongsville, Ohio 44149
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations, Electromagnetic propagation is affected by absorption and reflection
structures, objects and people.
a Field strengths from fixed transmitters, such as base station for radio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the
measured field strength in the location in which the Pulse Oximeter (RMI-POX2D) should be observed to verify normal
operation. If abnormal performance is observed, additional measurements may be necessary, such as reorienting of the
relocating the Pulse Oximeter (RMI-POX2D).
b Over the frequency range 150 kHz to 80 MHz, fields strengths should be less than 3 V/m
Recommended separation distances between portable and mobile RF communications equipment and
the EQUIPMENT or SYSTEMS - For all EQUIPMENT and SYSTEMS that are not LIFE-SUPPORTING
Recommended separation distances between
portable and mobile RF communications equipment and Pulse Oximeter (RMI-POX2D)
ALL RIGHTS RESERVED
Issue Date: 8/September 2011